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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04738929
Other study ID # EVCO
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 3, 2019
Est. completion date June 3, 2019

Study information

Verified date February 2021
Source Ankara City Hospital Bilkent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to compare acute effects of consuming extra virgin coconut oil (EVCO) as a source of medium chain fatty acids and extra virgin olive oil (EVOO) as a source of long chain fatty acids in normal weight and obese subjects.


Description:

Twenty male subjects (10 normal weight; 10 obese) consumed breakfast meals containing skimmed milk, fat-free white cheese, bread and EVCO (25 g) or EVOO (25 g). Visual analog scale evaluations, resting metabolic rate measurements and selected blood parameters analysis (glucose, triglyceride, insulin and plasma peptide YY) were performed before and after the test breakfast meals. In addition, energy intakes were evaluated by ad libitum lunch meal at 180 min.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 3, 2019
Est. primary completion date June 3, 2019
Accepts healthy volunteers No
Gender Male
Age group 19 Years to 40 Years
Eligibility Inclusion Criteria: - Metabolically healthy - Aged 19-40 years - Normal weight (BMI=18.5-24.9 kg/m²) and obese men (BMI=30-34.99 kg/m²) Exclusion Criteria: - smoking, - alcohol consumption, - weight gain/loss recently (> %5, in three months), - any genetic and metabolic diseases, - any food allergy/intolerance, - any medication, - restrained eating habits.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Extra virgin coconut oil or extra virgin olive oil
Subjects consumed standard breakfast meals containing "extra virgin coconut oil" or "extra virgin olive oil"

Locations

Country Name City State
Turkey Presidency of Republic of Turkey Health Center Ankara

Sponsors (2)

Lead Sponsor Collaborator
Ankara City Hospital Bilkent Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Energy expenditure change kcal 0, 60, 120, 180 minutes
Primary Subjective appetite feelings change visual analogue scales rating (0-10 cm) 0, 30, 60, 120, 180 minutes
Primary glucose change mg/dl 0, 30, 60, 120, 180 minutes
Primary insulin change mU/L 0, 30, 60, 120, 180 minutes
Primary peptide YY change pg/dl 0, 30, 60, 120, 180 minutes
Primary triglycerides change mg/dl 0, 30, 60, 120, 180 minutes
Primary Ad libitum energy intake kcal 180 minute
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